US2019275016A1PendingUtilityA1
NOVEL COMPOUNDS avB6 INTEGRIN ANTAGONISTS.
Assignee: GLAXOSMITHKLINE IP DEV LTDPriority: Sep 26, 2014Filed: May 28, 2019Published: Sep 12, 2019
Est. expirySep 26, 2034(~8.2 yrs left)· nominal 20-yr term from priority
Inventors:Niall Andrew AndersonMatthew Howard James Campbell-CrawfordAshley Paul HancockJohn Martin PritchardJoanna Mary Redmond
A61P 43/00A61P 35/00A61P 1/16A61P 13/12A61P 11/00C07D 471/04A61K 31/4375A61K 31/19A61K 9/0053
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Claims
Abstract
A compound of formula (I): being 4-(3-Fluoro-3-(2-(5, 6, 7, 8-tetrahydro-1, 8-naphthyridin-2-yl) ethyl) pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy) phenyl) butanoic acid, or a salt thereof.
Claims
exact text as granted — not AI-modified1 . A method of treating a cancer in a human in need thereof comprising administering to the human a therapeutically effective amount of (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid
or a pharmaceutically acceptable salt thereof.
2 . A method of treating a cancer in a human in need thereof comprising administering to the human a therapeutically effective amount of (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid citrate salt.
3 . The method according to claim 1 , where the cancer is selected from endometrial cancer, basal cell cancer, liver cancer, colon cancer, cervical cancer, oral cancer, pancreatic cancer, breast cancer, ovarian cancer, Kaposi's sarcoma, giant cell tumours, cancer associated with stroma, and solid tumours.
4 . The method according to claim 2 , where the cancer is selected from endometrial cancer, basal cell cancer, liver cancer, colon cancer, cervical cancer, oral cancer, pancreatic cancer, breast cancer, ovarian cancer, Kaposi's sarcoma, giant cell tumours, cancer associated with stroma, and solid tumours.
5 . A method of treating a cancer in a human in need thereof comprising administering a therapeutically effective amount to the human of a combination comprising (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid
or a pharmaceutically acceptable salt thereof, and a cancer therapy agent.
6 . A method of treating a cancer in a human in need thereof comprising administering a therapeutically effective amount to the human of a combination comprising (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid citrate salt and a cancer therapy agent.
7 . The method according to claim 5 , wherein the cancer is selected from endometrial cancer, basal cell cancer, liver cancer, colon cancer, cervical cancer, oral cancer, pancreatic cancer, breast cancer, ovarian cancer, Kaposi's sarcoma, giant cell tumours, cancer associated with stroma, and solid tumours.
8 . The method according to claim 6 , wherein the cancer is selected from endometrial cancer, basal cell cancer, liver cancer, colon cancer, cervical cancer, oral cancer, pancreatic cancer, breast cancer, ovarian cancer, Kaposi's sarcoma, giant cell tumours, cancer associated with stroma, and solid tumours.
9 . The method of claim 5 , wherein the cancer therapy agent is selected from chemotherapy, radiotherapy, targeted agents, immunotherapy, and cell or gene therapy.
10 . The method of claim 6 , wherein the cancer therapy agent is selected from chemotherapy, radiotherapy, targeted agents, immunotherapy, and cell or gene therapy.
11 . A combination comprising of (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid
or a pharmaceutically acceptable salt thereof, and a cancer therapy agent.
12 . A combination comprising of (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid citrate salt and a cancer therapy agent.
13 . A combination according to claim 11 , wherein the cancer therapy agent is selected from chemotherapy, radiotherapy, targeted agents, immunotherapy, and cell or gene therapy.
14 . A combination according to claim 12 , wherein the cancer therapy agent is selected from chemotherapy, radiotherapy, targeted agents, immunotherapy, and cell or gene therapy.
15 . A compound of formula (I) which is (S)-4-((S)-3-fluoro-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)-3-(3-(2-methoxyethoxy)phenyl)butanoic acid citrate salt.Join the waitlist — get patent alerts
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